Variant report

Variant rs6792479
Chromosome Location chr3:156921989-156921990
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:156905000-156922800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr3:156919400-156929000 Weak transcription Skeletal Muscle Female skeletal muscle
3 chr3:156919600-156922400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr3:156919600-156922400 Weak transcription Muscle Satellite Cultured Cells --
5 chr3:156919600-156922400 Weak transcription HUVEC blood vessel
6 chr3:156919600-156922400 Weak transcription NHDF-Ad bronchial
7 chr3:156919600-156928800 Weak transcription Primary T helper naive cells fromperipheralblood blood
8 chr3:156919800-156922200 Weak transcription Osteobl bone
9 chr3:156919800-156922400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr3:156919800-156922400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr3:156919800-156922400 Weak transcription Stomach Smooth Muscle stomach
12 chr3:156919800-156922600 Weak transcription Colon Smooth Muscle Colon
13 chr3:156920000-156922400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr3:156920000-156922400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr3:156920000-156922800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr3:156920200-156929600 Weak transcription Primary B cells from peripheral blood blood

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